Gene: LINC02476 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs143238378
rs143238378
LINC02476
1 1.000 0.120 7 119626216 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs150382487
rs150382487
LINC02476
1 1.000 0.120 7 119500548 intron variant T/A snv 2.4E-03 0.700 1.000 1 2019 2019
dbSNP: rs182830500
rs182830500
LINC02476
1 1.000 0.120 7 119521299 intron variant T/C snv 2.6E-03 0.700 1.000 1 2019 2019
dbSNP: rs188681640
rs188681640
LINC02476
1 1.000 0.120 7 119506105 intron variant A/G snv 2.4E-03 0.700 1.000 1 2019 2019